Skip to main content
Premium Trial:

Request an Annual Quote

Wisconsin Blood Supplier Using BioTrove's Genotyping Technology in Donor Matching

NEW YORK (GenomeWeb News) – The BloodCenter of Wisconsin is using BioTrove’s genotyping technology to develop a SNP-based screening tool that will help detect rare blood types and make for better transfusion matches, the company said today.
 
The BloodCenter, which provides blood to over 50 hospitals in Wisconsin, is using BioTrove’s OpenArray SNP platform in research that will allow it to stratify blood donors based on genotypic characteristics, which will improve speed and accuracy of transfusion, the company said.
 
“The need for blood is constant – and for those patients with rare blood types, finding a match can be extremely difficult,” Brad Pietz, director of product development for the diagnostic laboratories of the BloodCenter of Wisconsin, said in a statement.
 
Locating appropriate donors depends on more than matching the common blood type varieties A, B, and O, but it also depends on the specificity of antibodies in the recipient’s blood and antigens that may vary between individuals in the donor group.
 
The BioTrove platform uses through-hole nanoliter fluidics technology to allow researchers to conduct more than 3,000 simultaneous PCR analyses using a metal plate. In addition, the study with the BloodCenter will use chemistries from Applied Biosystems, which inked a genotyping collaboration with BioTrove in November 2007. 

The Scan

UK Pilot Study Suggests Digital Pathway May Expand BRCA Testing in Breast Cancer

A randomized pilot study in the Journal of Medical Genetics points to similar outcomes for breast cancer patients receiving germline BRCA testing through fully digital or partially digital testing pathways.

Survey Sees Genetic Literacy on the Rise, Though Further Education Needed

Survey participants appear to have higher genetic familiarity, knowledge, and skills compared to 2013, though 'room for improvement' remains, an AJHG paper finds.

Study Reveals Molecular, Clinical Features in Colorectal Cancer Cases Involving Multiple Primary Tumors

Researchers compare mismatch repair, microsatellite instability, and tumor mutation burden patterns in synchronous multiple- or single primary colorectal cancers.

FarGen Phase One Sequences Exomes of Nearly 500 From Faroe Islands

The analysis in the European Journal of Human Genetics finds few rare variants and limited geographic structure among Faroese individuals.